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ONTOLOGY REPORT - ANNOTATIONS


Term:Marsden Syndrome
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Accession:DOID:9008398 term browser browse the term
Synonyms:exact_synonym: Dystonia, familial, with visual failure and striatal lucencies;   Leber Hereditary Optic Neuropathy With Dystonia
 primary_id: MESH:C536024;   RDO:0001435
For additional species annotation, visit the Alliance of Genome Resources.


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Marsden Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mt-nd1 mitochondrially encoded NADH dehydrogenase 1 JBrowse link MT 2,740 3,694 RGD:8554872
G Mt-nd3 mitochondrially encoded NADH dehydrogenase 3 JBrowse link MT 9,451 9,798 RGD:8554872
G Mt-nd4 mitochondrially encoded NADH dehydrogenase 4 JBrowse link MT 10,160 11,537 RGD:8554872
G Mt-nd6 mitochondrially encoded NADH dehydrogenase 6 JBrowse link MT 13,543 14,061 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14759
    syndrome 4210
      Marsden Syndrome 4
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        sensory system disease 4231
          eye and adnexa disease 1971
            eye disease 1971
              optic nerve disease 183
                optic atrophy 86
                  Hereditary Optic Atrophies 57
                    Leber hereditary optic neuropathy 24
                      Marsden Syndrome 4
paths to the root